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Genome Editing Detection and Analysis Tools | Thermo Fisher Scientific - TW
Genome Editing Detection and Analysis Tools | Thermo Fisher Scientific - TW

TIDE: Tracking of Indels by DEcomposition
TIDE: Tracking of Indels by DEcomposition

CRISPR-Cas9 Genome Editing Guide – Finessing the technique and breaking new  ground - Behind the Bench
CRISPR-Cas9 Genome Editing Guide – Finessing the technique and breaking new ground - Behind the Bench

Precise CAG repeat contraction in a Huntington's Disease mouse model is  enabled by gene editing with SpCas9-NG | Communications Biology
Precise CAG repeat contraction in a Huntington's Disease mouse model is enabled by gene editing with SpCas9-NG | Communications Biology

A Survey of Validation Strategies for CRISPR-Cas9 Editing | Scientific  Reports
A Survey of Validation Strategies for CRISPR-Cas9 Editing | Scientific Reports

Netherlands Cancer Institute Grants Exclusive License to Desktop Genetics  for TIDE | Technology Networks
Netherlands Cancer Institute Grants Exclusive License to Desktop Genetics for TIDE | Technology Networks

Rapid Quantitative Evaluation of CRISPR Genome Editing by TIDE and TIDER |  SpringerLink
Rapid Quantitative Evaluation of CRISPR Genome Editing by TIDE and TIDER | SpringerLink

Inference of CRISPR Edits from Sanger Trace Data | bioRxiv
Inference of CRISPR Edits from Sanger Trace Data | bioRxiv

CRISPR-Cas9 vectors for genome editing and host engineering in the  baculovirus–insect cell system | PNAS
CRISPR-Cas9 vectors for genome editing and host engineering in the baculovirus–insect cell system | PNAS

Frontiers | Multiplexed Knockouts in the Model Diatom Phaeodactylum by  Episomal Delivery of a Selectable Cas9 | Microbiology
Frontiers | Multiplexed Knockouts in the Model Diatom Phaeodactylum by Episomal Delivery of a Selectable Cas9 | Microbiology

TIDE: Tracking of Indels by DEcomposition
TIDE: Tracking of Indels by DEcomposition

TIDER: Easy quantification of template-directed CRISPR
TIDER: Easy quantification of template-directed CRISPR

Splice donor site sgRNAs enhance CRISPR/Cas9-mediated knockout efficiency |  PLOS ONE
Splice donor site sgRNAs enhance CRISPR/Cas9-mediated knockout efficiency | PLOS ONE

TIDE: Tracking of Indels by DEcomposition
TIDE: Tracking of Indels by DEcomposition

TIDER: Easy quantification of template-directed CRISPR
TIDER: Easy quantification of template-directed CRISPR

TIDE: Tracking of Indels by DEcomposition
TIDE: Tracking of Indels by DEcomposition

Cells | Free Full-Text | A Versatile Strategy to Reduce UGA-Selenocysteine  Recoding Efficiency of the Ribosome Using CRISPR-Cas9-Viral-Like-Particles  Targeting Selenocysteine-tRNA[Ser]Sec Gene | HTML
Cells | Free Full-Text | A Versatile Strategy to Reduce UGA-Selenocysteine Recoding Efficiency of the Ribosome Using CRISPR-Cas9-Viral-Like-Particles Targeting Selenocysteine-tRNA[Ser]Sec Gene | HTML

TIDE: Tracking of Indels by DEcomposition
TIDE: Tracking of Indels by DEcomposition

Increasing CRISPR Efficiency and Measuring Its Specificity in HSPCs Using a  Clinically Relevant System: Molecular Therapy - Methods & Clinical  Development
Increasing CRISPR Efficiency and Measuring Its Specificity in HSPCs Using a Clinically Relevant System: Molecular Therapy - Methods & Clinical Development

TIDE
TIDE

CRISPR/Cas9-Directed Reassignment of the GATA1 Initiation Codon in K562  Cells to Recapitulate AML in Down Syndrome: Molecular Therapy - Nucleic  Acids
CRISPR/Cas9-Directed Reassignment of the GATA1 Initiation Codon in K562 Cells to Recapitulate AML in Down Syndrome: Molecular Therapy - Nucleic Acids

TIDE
TIDE

TIDE
TIDE